Catalyst for electrocatalytic carbon dioxide reduction reaction as well as preparation method and application of catalyst

A carbon dioxide, electrocatalysis technology, applied in electrodes, electrolysis process, electrolysis components, etc., can solve the problems of serious side reactions, insufficient catalytic performance, low product selectivity, etc.

Active Publication Date: 2021-09-17
BEIHANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, due to the low kinetics of the electrocatalytic carbon dioxide reduction reaction and the accompanying severe side reactions, catalysts for the carbon dioxide reduction reaction with both high catalytic activity and high selectivity are still the goal of current exploration.
[0003] Traditional electrocatalytic carbon dioxide reduction catalysts include Cu, Au, Ag and their alloys, which have relatively large defects in catalytic performance.
Although the recently emerging single-atom catalysts have relative advantages, they still have shortcomings in terms of catalytic performance, mainly reflected in the low selectivity of products at high current densities.

Method used

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  • Catalyst for electrocatalytic carbon dioxide reduction reaction as well as preparation method and application of catalyst
  • Catalyst for electrocatalytic carbon dioxide reduction reaction as well as preparation method and application of catalyst
  • Catalyst for electrocatalytic carbon dioxide reduction reaction as well as preparation method and application of catalyst

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preparation example Construction

[0036]The present invention also provides a method for preparing a catalyst for the electrocatalytic carbon dioxide reduction reaction described in the above technical solution, comprising the following steps:

[0037] mixing sodium chloride, glucose, nickel acetate tetrahydrate, boric acid and water, and freeze-drying to obtain a precursor;

[0038] The precursor is carbonized and calcined in sequence to obtain the catalyst for the electrocatalytic carbon dioxide reduction reaction.

[0039] In the present invention, unless otherwise specified, the raw materials used in the present invention are preferably commercially available products.

[0040] In the invention, sodium chloride, glucose, nickel acetate tetrahydrate, boric acid and water are mixed and freeze-dried to obtain a precursor.

[0041] In the present invention, the mass ratio of the sodium chloride, glucose, nickel acetate tetrahydrate and boric acid is preferably 10000:750:12:(20-40), more preferably 10000:750:1...

Embodiment 1

[0059] Dissolve sodium chloride (10 g), glucose (0.75 g), boric acid (30 mg) and nickel acetate tetrahydrate (12 mg) in 80 mL of deionized water, and freeze at -50 °C for 12 h; The material was dried at -50°C and 1Pa for 48 hours to sublimate the ice to obtain the precursor. Afterwards, the above-mentioned precursor was placed in a high-temperature tube furnace, and the temperature was raised to 240 °C at 10 °C / min in an atmosphere of argon, and then continued to be heated at 10 °C in a mixed atmosphere of ammonia and argon at a volume ratio of 1:4. °C / min to 400 °C; then continue to heat up to 700 °C at 10 °C / min under an atmosphere of argon, and then keep warm for 30 min in a mixed atmosphere of ammonia and argon with a volume ratio of 1:4, then in argon The atmosphere was kept for 1.5h; then the temperature was raised to 1000°C at 20°C / min under the atmosphere of argon, and the temperature was kept for 1h to obtain the catalyst, which was named as BNC-SANi.

[0060] As mea...

Embodiment 2

[0088] The difference with Example 1 is: the quality of boric acid is 40mg. As measured by XPS, the mass of nickel single atom in the obtained catalyst is 2.40% of the mass of the carbon skeleton, the mass of the nitrogen atom is 13.49% of the mass of the carbon skeleton; the mass of the boron element is 8.61% of the mass of the carbon skeleton.

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Abstract

The invention belongs to the technical field of catalyst preparation, and provides a catalyst for electrocatalytic carbon dioxide reduction reaction as well as a preparation method and application thereof. According to the catalyst disclosed by the invention, a boron element is doped on a three-dimensional porous carbon skeleton, and the boron element, a nitrogen atom and a nickel metal single atom form a Ni-N4B2 active site, that is, the doping of the boron element changes a coordination environment of the center of the active site; therefore, the catalyst improves the Faraday efficiency of the product of the Ni-N4 site under high current density in the electrocatalysis carbon dioxide reduction process. Data of the embodiment show that when the catalyst obtained in the embodiment 1 is loaded on a gas diffusion electrode, the current density of the catalyst reaches 213 + / -30mA. Cm <-2 > under the potential of-1.2 V, and the Faraday efficiency of the product carbon monoxide under the potential reaches up to 97.37%.

Description

technical field [0001] The invention relates to the technical field of catalyst preparation, in particular to a catalyst for electrocatalytic carbon dioxide reduction reaction and its preparation method and application. Background technique [0002] The reduction of carbon dioxide to chemical feedstocks via electrocatalysis offers a promising strategy for promoting global carbon balance. However, due to the low kinetics of the electrocatalytic CO2 reduction reaction and the accompanying severe side reactions, catalysts for the CO2 reduction reaction with both high catalytic activity and high selectivity are still the goal of current exploration. [0003] Traditional electrocatalytic carbon dioxide reduction catalysts include Cu, Au, Ag and their alloys, which have relatively large defects in catalytic performance. Although the recently emerging single-atom catalysts have relative advantages, they still have shortcomings in terms of catalytic performance, mainly reflected in...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C25B11/091C25B11/032C25B3/26C25B3/07
CPCC25B11/091C25B11/032C25B3/26C25B3/07
Inventor 宫勇吉古小康翟朋博
Owner BEIHANG UNIV
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